BIOL 160: General Biology
Definition Worksheet #9: Chapter 8
Define the following terms related to cellular respiration.
1. Absorptive State The period which the gastroinestestinal tract is full and the anabolic processes exceed catabolism.
2. Aerobic Respiration Metabolic pathaway that breaks down carbohydrates to produce ATP by using oxygen.
3. Alcohol Fermentation An aerobic pathaway that breaks down glucose, forms ethanol and ATP. Begins with glycolysis, end reaction on regenerate NAD+ so glycolysis continue
4. Anaerobic Respiration: A way for an organism to produce usable energy without the involvement of oxygen; respiration without oxygen.
5. Cellular Respiration: Biochemical pathaway by which cells release energy from the chemical bonds of food molecules and provide energy for the essential process of life.
6. Electron Transport Chain: Array of enzymes and other molecules in a cell membrane that accept and give up electrons in sequence releasing the energy of the electronsin small usable incraments.
7. Glucose: A hexon monosacharide that is the primary energy source for body cells.
8. Glycogen: A polysacharide that is the storage form for excess glucose in the liver and muscles.
9. Glycolysis: first stage of the aerobic respiration and fermentation; glucose or another sugar molecule is broken down to 2 pyruvate for a net yield of 2 ATP.
10. Kreb's Cycle: The second stage of aerobic respiratioin; breaks down 2 pyruvate to CO2 and H2O for a net yield of 2 ATP and reduced enzymes.
11. Lactic Acid Fermentation: Biological process by which sugars and glucose fructoses and sucrose are converted into cellular energy and the metabolic by product lactate. It's the anaerobic form of respiration that occurs in some bacteria and animal cells. such as muscle cells, in the absence of oxygen.
12. NADH Nicotinamide adenine dinucleotide, abbreviation NAD+ a coenzyme found in all living cells. The compound is a dinucleotide, since it consists of 2 nucleotides joined through their phosphate groups with one nucleotide containing an adenine base and the other containing nicotinamide. FADH2 Adds its electrons to the electron transport system at a lower level than NADH, so it produces 2 ATP.
13. Oxidative Phosphorylation A metabolic pathaway that uses energy released by the oxidation of nutrient to produce ATP.
14. Post-Absorptive State The period of time when nutrients are not being absorbed from the digestive system and the body must rely on internal energy reserves. Main reactions in this time are classified as catabolic.
15. Pyruvate The end product of glycolysis.
16. Substrate-level Phosphorylation Type of chemical reaction that results in the formation and creation of ATP by the direct transfer and donation of phophoryl group to ADP from a reactive intermediate.
CHAPTER 8: How Cells Release Stored Energy
1. All living organisms, regardless of how small use energy on a regular basis. So where do they get the energy?
A. Plants (also known as producers) make ATP during the process of photosynthesis and then use that energy to drive chemical reactions that convert CO2 and H2O into glucose (C6H12O6) which most of them store as the large complex
carbohydrate molecules called Polysacharides. (Remember from module 2?).
B. Humans get their energy second or third hand from eating plants or other animals that have eaten the plants. Regardless of the source, the body ultimately converts the energy stored in carbohydrates, lipids and proteins back into the form of ATP molecules that the cells can use on the molecular level.
2. There are two main types of energy-releasing pathways used by cells:
A. ANAEROBIC_ Pathway: this method of producing energy evolved first. It occurs in the cytoplasm of the cell and does NOT require oxygen. Many prokaryotes (bacteria) still live in places where there is a very limited oxygen supply and still rely on this pathway for producing energy. There are also times when the oxygen supply to some cells in the body is not great enough to meet the cellular demands for energy so cells must rely on this method as well.
B. AEROBIC_ Pathway: this method evolved later and is the main pathway used by the cells in the body to produce the needed energy. This pathway requires an adequate supply of oxygen to operate successfully and begins
in the cytoplasm but continues in the MITOCHONDRIA. The pathway is divided into three parts or stages: 1.GLYCOLYSIS: occurs in the cytoplasm and involves a series of reactions that breaks a glucose molecule into two smaller pyruvate (pyruvic acid) molecules and in the process also produces 2 ATP molecules. 2._KREBS CYCLE: occurs in the inner membrane spaces (matrix) of the mitochondria and involves a series of reactions that removes all remaining hydrogen atoms with their electrons from the carbon chain and in the process also produces 6 CO2 and 2 ATP molecules. 3. _ELECTRON TRANSFER_PHOSPHORYLATION: occurs along the inner mitochondrial membrane and involves a series of chemical reactions that remove the electrons from the hydrogen atoms and uses the potential energy of a concentration gradient to drive the production of ATP molecules and in the process produces 6 H2O and 32-34 ATP molecules.
3. Overview of Aerobic (Cellular) Respiration:
http://www.mansfield.ohio-state.edu/~sabedon/biol1100.htm
Great link that has details about respiration PLUS a very succinct energy accounting!!!
A. Aerobic respiration starts with 1 glucose molecule and produces a total
energy yield of 36 ATP or more.
B. The following is the overall chemical reaction for cellular respiration:
1 C6H12O6 + 6 O2 → 6 CO2 + 6 H2O + 36 ATP Glucose + Oxygen → Carbon dioxide + Water + Energy
C. The overall process involves over 30 different reactions producing specific intermediate molecules along the way. You will NOT need to remember all of these by name, only a few very select molecules.
D. Each chemical reaction requires a specific enzyme (you don’t need to know these by name either) and several very important co-enzymes (NAD+ and FAD) that function to “carry” the Hydrogen atoms to the final stage of the pathway. Because of their function, these coenzymes are often called “carrier” or “transport” molecules.
4. Glycolysis_: The First Stage of cellular respiration (the Energy- releasing Pathway).
These reactions take place entirely in the cytoplasm and occurs in two stages: A. Energy releasing Steps:
Two ATP molecules found in the
cytoplasm of the cell are used to activate
the incoming glucosemolecule and in a sense “traps” it in the cell to ensure the concentration gradient is maintained and to rearrange the molecule to make it more symmetrical (balanced) so it will be easier to break in half.
B. Energyreleasing_ Steps: The product of the first stage is split into two three-carbon molecules called PGAL that are further modified by removing a hydrogen atom from each and transferring them to two NAD molecules formingNADH_
and replacing the hydrogen atoms with
two phosphate groups. Eventually the
phosphate groups are removed and
transferred to ADP molecules forming a
total of four ATPmolecules and two molecules of pyruvate (pyruvic acid) as the end products of this series of reactions. The PGAL molecules are important intermediate molecules as they serve as a location where part of the triglyceride molecules can enter the pathway to be used to produce ATP energy. And the 2PGA or BPG molecules are important as they influence whether hemoglobin molecules in red blood cells will keep or release oxygen to the tissue. When ATP molecules are produced in the absence of oxygen by transferring phosphate groups from the substrate molecules (reactants) to ADP molecules, the process is calledsubstrate-level PHOSPHORYLATION.
In review: The following are the key points to remember about Glycolysis.
The initial reactant was Glucose. Two molecules of ATP were added helping to trap and rearrange the molecule to make it easier to break
in half. Eventually 4 ATP molecules were produced, resulting in a net gain
overall of 2ATP, and2NADH molecules (to be used later by the mitochondria to produce even more ATP) as well as two molecules of the final product. These series of reactions do not rely on the presence of oxygen, so they can occur in an anaerobic situation when oxygen levels are low. 5. KrebsCYCLE (Citric Acid Cycle): The Second Stage of cellular respiration (the Energy-releasing Pathway). These reactions take place entirely in the inner compartment or inner membrane space (matrix) of the mitochondria and also occur in two stages: A. The Acetal Coa Formation Stage: Remember that Glycolysis ended with the
production of 2 pyruvate (pyruvic acid)
molecules; therefore all reactions in this step are
doubled. The pyruvate molecules are oxidized into
two 2-carbon molecules with the help of a special
enzyme helper called “Coenzyme A” producing two
molecules of Acetyl Co-A. In the process, a total of
another 2NADH molecules were produced as well as 2 CO2 molecules that are waste products. B. KREBS CYCLE proper:
Because there were two Acetyl-CoA molecules
produced in preparing to enter the cycle, all
reactions here are also doubled. The remaining hydrogen atoms are removed and given to the “carrier molecules” NAD+ and FAD producing an additional 6 NADH and 2 FADH2 molecules that will later be used by the mitochondria to produce even more ATP molecules. In addition to the “carrier molecules” produced, an additional 4
CO2 molecules and 2 ATP are
produced by a process called substrate-level
phosphorylation.
Even though these series of reactions do not rely on the presence of oxygen directly, the main products produced (NADH and FADH2) will be sent to the last stage of cellular respiration that DOES require oxygen and therefore Krebs Cycle will only occur in an aerobic situation when oxygen levels are high.
In review: The following are the key points to remember about Krebs Cycle.
The process began with two molecules of pyruvates that were produced by the break-down of one glucose molecule so all reactions are actually doubled (once for each of these molecules). In the initial reactions,
two hydrogen atoms were removed forming two molecules of and
two molecules of NADHthat are waste products, as well as two molecules ofCO2that will enter Krebs cycle proper. During the final series of reactions,2more NADH will be produced for a total of6NADH,2 FADH2, four more molecules of co2 that are waste products for a total of 6 CO2 as well as 2ATP by a process called substrate-level phosphorylation.
6.oxidative PHOSPHORYLATION: The third Stage of cellular respiration (the Energy-releasing Pathway), is also known as the electron transport chain (since it involves the removal of electrons from the hydrogen atoms), or oxidative phosphorylation (since oxygen is required to make ATP).
A. These reactions takes place along the inner-mitochondrial membrane. The coenzyme carrier molecules NADH and FADH2 deliver the Hydrogen atoms to specialized enzymes (embedded in the membrane) that will remove the electrons
and use the potential energy to drive the production of ATP molecules.
B. The “Chemiosmosis Theory” attempts to explain how this process occurs.
1. When the hydrogen atoms are delivered to the specialized enzymes in the membrane, the enzymes remove the electron and as it is passed along from enzyme to enzyme the action produces enough energy to transfer the unbound hydrogen ions (H+1) to the outer compartment of the mitochondria creating a concentration gradient of hydrogen ions.
2. Also embedded in the inner-mitochondrial membrane are very specialized
transporter (channel) proteins called ATP synthase that allow the Hydrogen ions (H+1) that have a high concentration in the outer compartment to move down their concentration gradient into the inner compartment. The movement of the H+1 ions through these proteins provides the needed energy to drive the phosphorylation of ADP into ATP.
3. At the end of the electron transport system the electrons need to go somewhere. Remember from chapter 2 that some elements are “takers” of
electrons and some are “givers”. The element oxygen was classified as a taker . Oxygen atoms take the electrons from the transporter enzymes becoming a negative ion (O-2) at which point it is immediately attracted to some of the hydrogen ions (H+1) and the two join together to produce a molecule of water . To put it another way, oxygen
is the final electron acceptor and water is the final product along with the ATP molecules. 7. Anaerobic Energy-Releasing Pathways: A. Unlike aerobic respiration, the anaerobic pathways do not use oxygen in the last steps as the final electron acceptor; their final steps have the important function of regenerating NAD+ “carrier molecules. 1. Without an adequate supply of oxygen there would be no place for the electrons to go, so the electrons would “build up” in the electron transport chain, and soon the NADH and FADH2 would not be able to release their Hydrogen atoms, essentially shutting down this stage. 2. If the carrier molecules were not able to release the hydrogen, soon there would be no more available to “take” the hydrogens released in Krebs cycle, essentially shutting down that stage as well. 3. If Krebs cycle “shuts down” it seems logical that Glycolysis would shut down as well; however, the cell must have at least some ATP to stay alive! B. Without an adequate supply of oxygen, only the first stage (Glycolysis) can occur. Each glucose molecule will produce a total of only 2ATP rather than 36 ATP when oxygen is readily available. This is not a very good use of glucose but 2 ATP molecules are better than none and this works fine for a short time. The problem is that the NADH produced have no where to go (remember the electron transfer chain is shut down without oxygen) and will eventually need to be recycled. C. There are two processes that can recycle the NADH back into NAD+1. 1.Alcohol FERMENTATION:
a. This process is used by yeast and other anaerobic organisms to produce energy when oxygen levels are low.
b. This process also uses Glycolysis as the first step to produce 2 ATP, but the rest of the energy-releasing pathways are shut down so because there is no place to send the Pyruvic acid molecules, and the supply of NADH will run out, the cell uses these molecules to produce Carbon dioxide gas and Ethanol (ethyl alcohol). c. Yeast is used in baking bread because the yeast uses this form of respiration for their energy supply and in the process produce CO2 which is what causes the bread to rise.
d. Ethanol in large quantities is toxic and eventually the cells will die, which is why this method is NOT used by our bodies to generate more NAD+ when oxygen levels are low.
2. Lactate FERMENTATION:
a. This process occurs especially in muscle cells when the demand for energy is intense but brief, as in sprinting or lifting weights.
b. Special enzymes remove the hydrogen atoms from the NADH and give it back to the pyruvate molecule converting it into a lactate (lactic acid) molecule, and in the process the NAD+ is regenerated so glycolysis can continue. c. It is not the most efficient use of glucose and as the supply of glucose is depleted the muscle will fatigue (get tired) and lose their ability to contract.
d. Some muscle cells (muscle fibers) must be able to stay contracted for a long period of time to keep the body or body part upright, such as your back and neck muscles or be able to contract repeatedly for an extended period of time, as in the leg muscles of marathon runners. Cells capable
of these activities are called slow twitchmuscle fibers, and make ATP only by aerobic respiration. This means they must have a large number of mitochondria , and a constant supply of oxygen. Muscles containing this type of cells appear dark in color due to the increased blood supply and the presence of a protein that stores the oxygen until needed, hence the term “dark” meat.
e. Some muscle cells (muscle fibers) must be able to contract very quickly and forcefully, as in jumping, throwing a “fast pitch” ball or a reflex reaction as when touching a hot object. Cells capable of these activities
are called fast twitch muscle fibers, and use the process of Lactate Fermentation (anaerobic respiration) to make ATP; therefore these cells have very few mitochondria. The pathway makes ATP very quickly but not for very long. It is not an effective use of glucose (2 ATP verses 36 ATP). Muscles containing this type of cells do not have a rich blood supply and do not store oxygen, so appear light in color, hence the term “light” or “white” meat.
8. Alternative Energy Sources in the Human Body
A. This chapter has concentrated on the use of glucose for the production of ATP energy because it is the body’s preference as an energy source. When glucose levels are high, the cell makes as much ATP as possible to have it available if the cell should need it in the future. Once the ATP levels get high enough (especially in the muscle and liver cells), the glucose is used to make other molecules like glycogen and triglycerides to store the energy for later use.
1. Energy from GLYCOGEN stored in the liver and skeletal muscles:
a. When blood sugar levels decline, the pancreas releases the hormone glucagon (glucose is almost gone).
b. Liver cells are stimulated to break down the glycogen back into glucose and release it to the blood. Muscle cells are also stimulated to break down the glycogen, but they keep the glucose for themselves and do not release it into the blood.
c. Polysaccharides like glycogen and starch have the potential of generating 4 kilocalories of energy per gram.
2. Energy from FATS (Triglycerides) stored in adipose cells:
a. The triglycerides are broken down into their component parts:
1. The 3-carbon glycerol backbone enters at the half-way point of glycolysis and continues through the rest of the cellular respiration pathways as though it started out as glucose.
2. The fatty acid molecules (tails) are broken down with the help of a
coenzyme into acetyl-Co A molecules that enter Krebs cycle
and continue through the rest of the cellular respiration pathways as though they started out as glucose.
b. Fats have a much higher concentration of hydrogen atoms than carbohydrates and proteins and therefore more electrons and more energy potential.
c. They are also much less dense (are lighter) so gram for gram fats have the potential of generating more than twice the amount of energy as either carbohydrates or proteins, in fact fats have the potential of generating
9 kilocalories per gram.
3. Energy from Proteins:
a. The proteins are first broken down into their monomers (building blocks)
called Amino Acids. b. The amino functional group is removed from the carbon atoms and excreted from the body as part of urine. c. The carbon fragment that remains generally enters somewhere in kreb cycle , depending on the number of carbon atoms in the group and continues through the pathway as though it started out as glucose. d. Proteins like carbohydrates are able to produce 4 kilocalories of energy per gram. B. During any 24-hour period, the body experiences two broad patterns of metabolic activity: the absorptive state and the postabsorptive state. 1. ABSORPTIVE STATE of metabolism: this is the period of time after consuming a meal (about 4 hours) when the body is absorbing nutrients from the digestive system. Some of the monomers are used immediately for energy; however the vast majority is stored for future use between meals, like when we are sleeping. The main reactions occurring at this time are classified as_(the building of large molecules from small ones) for growth of tissue and storage of energy reserves for future use. 2. POSTABSORPTIVE STATE of metabolism: this is the period of time when nutrients are NOT being absorbed from the digestive system and the body must rely on internal energy reserves. The main reactions occurring at this time are classified as___ (the breaking down of large molecules into smaller ones). Generally during this time, the goal is to maintain energy levels in the body. The glucose supply has dropped significantly so the body shifts from glucose catabolism to fatty acid and protein catabolism to obtain energy.
9. Just a few more points that need to be emphasized, then you’re done!
A. The overall reaction of cellular respiration is
1 C6H12O6 + 6 O2 → 6 CO2 + 6 H2O + 36 ATP
however no chemical reaction is ever 100% efficient. Our bodies are only able to capture about 40% of the total potential energy stored in a glucose molecule; the rest is lost as heat. This is why when you exercise, your cells need more energy so the rate of cellular respiration increases and more heat is produced, your body begins to overheat and you start sweating to try to lower the body temperature.
B. The energy-releasing pathways discussed in this chapter are also known as CELLULAR RESPIRATION. It is called this because the word respiration means the exchange of gases. The respiratory system in the body is responsible for taking in oxygen from the air and releasing carbon dioxide produced by the body. It has been shown that oxygen is critical to the efficient production of ATP from glucose, so cells must take in oxygen from the blood and use it to make ATP. It has also been shown that CO2 is produced as a waste product and the cell must eliminate it so in a sense the cells are “breathing” or exchanging gases just like the lungs.
C. All molecules (chemicals) have stored potential energy in the electrons located in their bonds. The goal of cellular respiration is to get at those electrons and use them to drive the production of ATP. To capture the electrons, hydrogen atoms must be separated from the carbon and oxygen so bonds must be broken, which releases heat. Remember, the hydrogen atom is the “weakest” of all the atoms in keeping the electron so it is the target of cellular respiration; if some other element was keeping the electron it may not give it back. The carrier molecules NAD+ and FAD are responsible for making sure the Hydrogen (with the electron) make it to their final destination (the electron transport chain).
D. Any substance that loses a hydrogen (or electron) is being OXIDIZED. Therefore glucose and all the intermediate molecules are being oxidized. Each of these molecules is losing some of their potential energy each time they lose or give away a hydrogen atom. The “carrier molecules” NAD+ and FAD are being REDUCED when they take the hydrogen atoms, which means they are “absorbing” more potential energy until they release the electron at the electron transport chain. The oxygen atom is the final electron acceptor, so it also is described as being REDUCED in the process of cellular respiration. Remember, any time a bond is formed, the substance is being REDUCED (more potential energy) and any time a bond is breaking, the substance is being OXIDIZED (less potential energy).
REVIEW ACTIVITIES:
10. Glycolysis is the first of three steps in cellular respiration. Review glycolysis by matching each phrase on the right with a term on the left. Some terms are used twice.
_ 1. Compound formed between glucose and pyruvic acid
_ 2. Not involved in glycolysis
_ 3. Fuel molecule broken down in glycolysis
_ 4. Produced by substrate-level phosphorylation
_ 5. Invested to energize glucose molecule at start of process
_ 6. Reduced as glucose is oxidized
_ 7. Glucose converted to two molecules of this
_ 8. Assembled to make ATP
_ 9. “Splitting of sugar”
_ 10. Carries hydrogen and electrons from oxidation of
glucose
A. NADH
B. Pyruvic acid
C. ATP
D. NAD+
E. Glucose
F. Glycolysis
G. ADP and P
H. Oxygen
I. Intermediate
11. Check your overall understanding of cellular respiration by matching each of the phrases below with one of the stages of the process. Assume in each case that you originally started with one glucose molecule. (Some may require more than one letter.)
A. Glycolysis
B. Krebs’ Cycle and the Preparatory Steps
C. Electron Transport Chain (oxidative phosphorylation)
D. Lactic Acid Fermentation
_ 1. Generates most of the ATP formed by cellular respiration
_ 2. Begins the oxidation of glucose
_ 3. Occurs outside the mitochondrion
_ 4. Oxygen combines with H+ to form water molecules.
_ 5. Oxidizes NADH and FADH2, producing NAD+ and FAD
_ 6. Pyruvate is a reactant.
_ 7. Where electrons and hydrogen combine with O2 to form H2O
_ 8. Occurs along the inner mitochondrial membrane
_ 9. Generates most of the CO2 produced by cellular respiration
_ 10. FADH2 and NADH deliver hydrogen ions and electrons to this stage.
_ 11. ATP synthase makes ATP.
_ 12. Reduces NAD+ and FAD, producing NADH and FADH2
_ 13. Oxidative phosphorylation occurs to form ATP molecules.
_ 14. The carbon atoms in pyruvate leave as CO2 molecules.
_ 15. Oxidation and reduction reactions occur.
_ 16. Coenzyme A binds to a two-carbon acetyl group.
_ 17. Two NAD+ molecules form in the absence of oxygen.
_ 18. Two FADH2 and ten NADH are sent to this stage
_ 19. Lactic acid is an end product
_ 20. Water is one of the major products
_ 21. Occurs within the mitochondrion
_ 22. Two FADH2 and eight NADH form.
_ 23. Hydrogen ions collect in the mitochondrion’s outer compartment.
_ 24. Hydrogens and electrons are transferred to NAD+ and FAD.
_ 25. Two ATP molecules form by substrate-level phosphorylation. _ 26. Oxygen is a major reactant
_ 27. No oxygen is required for ATP to be produced.
_ 28. Thirty-two to thirty-four ATPs are produced.
_ 29. NAD+ → NADH
_ 30. Carried out by enzymes in the matrix (fluid) of the mitochondrion
12. Choose the one most appropriate answer for each.
A. Starting point for three energy-releasing pathways
B. The overall process by which cells use oxygen to make the vast majority of the ATP needed
C. Site of glycolysis
D. Third and final stage of aerobic respiration; highest ATP yield generated
E. Oxygen is not the final electron acceptor
F. Catalyze each reaction step in the energy-releasing pathways
G. Second stage of aerobic respiration; pyruvate is broken down to CO2 and H2O
H. Site of the aerobic pathway
I. The final electron acceptor in aerobic pathways
J. The energy form that drives metabolic reactions
13. Compare the two mechanisms that generate ATP in cellular respiration—oxidative phosphorylation and substrate-level phosphorylation.
A. In what stage(s) of cellular respiration does each occur?
B. Where does each get the energy for making ATP?
C. Which one produces the most ATP under aerobic conditions?
D. Which one produces the most ATP under anaerobic conditions?
Sample test questions for chapter 8:
1. Cellular respiration oxidizes sugar and produces ATP in three main stages:
a. diffusion, passive transport and active transport
b. glycolysis, lactic acid fermentation, alcoholic fermentation
c. Krebs cycle, acetyl CoA, ATP
d. Glycolysis, Krebs cycle, electron transport chain
2. During “REDOX” reactions
a. the loss of electrons from one substance is called reduction
b. a substance that gains electrons is said to be oxidized
c. electrons are lost from one substance and added to another substance
d. protons from one molecule replace the electrons lost from another molecule
e. A, B and C
3. Which of the following statements differentiates substate-level phosphorylation from chemiosmotic (oxidative) phosphorylation?
a. a phosphate group is transferred directly from a metabolic intermediate to ADP forming ATP
b. it does not require the electron transport chain
c. it can occur in the absence of oxygen
d. it can occur outside the mitochondria
e. all of the above
4. During which of the following phases of cellular respiration does substrate-level phosphorylation take place?
a. glycolysis
b. the Krebs cycle
c. electron transport chain
d. both A and B
5. The end products of glycolysis include
a. FADH2
b. NADH
c. Acetyl CoA
d. glucose
e. CO2
6. In the respiratory electron transport chain, electrons pass from one electron transport molecule to another and are finally accepted by
a. a molecule of CO2
b. a molecule of water
c. an oxygen atom
d. ADP
e. ATP
7. When a fatty acid molecule is used for aerobic respiration, it is converted into , which is fed into. a. glucose……..glycolysis b. glyceraldehyde-3-phosphate…….glycolysis (partway through) c. acetyl CoA…….the Krebs cycle
8. The body’s preferred source of energy is/are a. triglycerides b. proteins c. glycerol d. macrominerals e. glucose
9. The end product(s) of the electron transport chain is/are a. ATP b. ATP and CO2 c. pyruvic acid d. ATP and water e. ATP and O2
10. Each NADH is capable of producing how many ATP from the Electron Transport Chain? a. 1 b. 2 c. 3 d. 30 e. 36
11. Under anaerobic conditions, muscle cells produce __ from the glucose as it is producing ATP energy.
a. ethyl alcohol
b. pyruvate
c. lactic acid
d. glycogen
12. Which of the following processes occurs inside the mitochondria?
a. Kreb’s Cycle
b. Electron Transport Chain
c. Glycolysis
d. A and B
e. A, B and C
13. In which of the following processes does substrate level phosphorylation occur?
a. Kreb’s Cycle
b. Glycolysis
c. Electron Transport Chain
d. A and B
e. A, B and C
14. Most of the ATP is produced
a. by substrate level phosphorylation
b. by oxidative phosphorylation
15. Which has the potential of producing the most ATP?
a. glucose
b. amino acid
c. fatty acid
Definition Worksheet #9: Chapter 8
Define the following terms related to cellular respiration.
1. Absorptive State The period which the gastroinestestinal tract is full and the anabolic processes exceed catabolism.
2. Aerobic Respiration Metabolic pathaway that breaks down carbohydrates to produce ATP by using oxygen.
3. Alcohol Fermentation An aerobic pathaway that breaks down glucose, forms ethanol and ATP. Begins with glycolysis, end reaction on regenerate NAD+ so glycolysis continue
4. Anaerobic Respiration: A way for an organism to produce usable energy without the involvement of oxygen; respiration without oxygen.
5. Cellular Respiration: Biochemical pathaway by which cells release energy from the chemical bonds of food molecules and provide energy for the essential process of life.
6. Electron Transport Chain: Array of enzymes and other molecules in a cell membrane that accept and give up electrons in sequence releasing the energy of the electronsin small usable incraments.
7. Glucose: A hexon monosacharide that is the primary energy source for body cells.
8. Glycogen: A polysacharide that is the storage form for excess glucose in the liver and muscles.
9. Glycolysis: first stage of the aerobic respiration and fermentation; glucose or another sugar molecule is broken down to 2 pyruvate for a net yield of 2 ATP.
10. Kreb's Cycle: The second stage of aerobic respiratioin; breaks down 2 pyruvate to CO2 and H2O for a net yield of 2 ATP and reduced enzymes.
11. Lactic Acid Fermentation: Biological process by which sugars and glucose fructoses and sucrose are converted into cellular energy and the metabolic by product lactate. It's the anaerobic form of respiration that occurs in some bacteria and animal cells. such as muscle cells, in the absence of oxygen.
12. NADH Nicotinamide adenine dinucleotide, abbreviation NAD+ a coenzyme found in all living cells. The compound is a dinucleotide, since it consists of 2 nucleotides joined through their phosphate groups with one nucleotide containing an adenine base and the other containing nicotinamide.
FADH2 Adds its electrons to the electron transport system at a lower level than NADH, so it produces 2 ATP.
13. Oxidative Phosphorylation A metabolic pathaway that uses energy released by the oxidation of nutrient to produce ATP.
14. Post-Absorptive State The period of time when nutrients are not being absorbed from the digestive system and the body must rely on internal energy reserves. Main reactions in this time are classified as catabolic.
15. Pyruvate The end product of glycolysis.
16. Substrate-level Phosphorylation Type of chemical reaction that results in the formation and creation of ATP by the direct transfer and donation of phophoryl group to ADP from a reactive intermediate.
CHAPTER 8: How Cells Release Stored Energy
1. All living organisms, regardless of how small use energy on a regular basis. So where do they get the energy?
A. Plants (also known as producers) make ATP during the process of photosynthesis and then use that energy to drive chemical reactions that convert CO2 and H2O into glucose (C6H12O6) which most of them store as the large complex
carbohydrate molecules called Polysacharides. (Remember from module 2?).
B. Humans get their energy second or third hand from eating plants or other animals that have eaten the plants. Regardless of the source, the body ultimately converts the energy stored in carbohydrates, lipids and proteins back into the form of ATP molecules that the cells can use on the molecular level.
2. There are two main types of energy-releasing pathways used by cells:
A. ANAEROBIC_ Pathway: this method of producing energy evolved first. It occurs in the cytoplasm of the cell and does NOT require oxygen. Many prokaryotes (bacteria) still live in places where there is a very limited oxygen supply and still rely on this pathway for producing energy. There are also times when the oxygen supply to some cells in the body is not great enough to meet the cellular demands for energy so cells must rely on this method as well.
B. AEROBIC_ Pathway: this method evolved later and is the main pathway used by the cells in the body to produce the needed energy. This pathway requires an adequate supply of oxygen to operate successfully and begins
in the cytoplasm but continues in the MITOCHONDRIA . The pathway is divided into three parts or stages:
1. GLYCOLYSIS: occurs in the cytoplasm and involves a series of reactions that breaks a glucose molecule into two smaller pyruvate (pyruvic acid) molecules and in the process also produces 2 ATP molecules.
2. _KREBS CYCLE: occurs in the inner membrane spaces (matrix) of the mitochondria and involves a series of reactions that removes all remaining hydrogen atoms with their electrons from the carbon chain and in the process also produces 6 CO2 and 2 ATP molecules.
3. _ELECTRON TRANSFER_PHOSPHORYLATION: occurs along the inner mitochondrial membrane and involves a series of chemical reactions that remove the electrons from the hydrogen atoms and uses the potential energy of a concentration gradient to drive the production of ATP molecules and in the process produces 6 H2O and 32-34 ATP molecules.
3. Overview of Aerobic (Cellular) Respiration:
http://www.mansfield.ohio-state.edu/~sabedon/biol1100.htm
Great link that has details about respiration PLUS a very succinct energy accounting!!!
A. Aerobic respiration starts with 1 glucose molecule and produces a total
energy yield of 36 ATP or more.
B. The following is the overall chemical reaction for cellular respiration:
1 C6H12O6 + 6 O2 → 6 CO2 + 6 H2O + 36 ATP
Glucose + Oxygen → Carbon dioxide + Water + Energy
C. The overall process involves over 30 different reactions producing specific intermediate molecules along the way. You will NOT need to remember all of these by name, only a few very select molecules.
D. Each chemical reaction requires a specific enzyme (you don’t need to know these by name either) and several very important co-enzymes (NAD+ and FAD) that function to “carry” the Hydrogen atoms to the final stage of the pathway. Because of their function, these coenzymes are often called “carrier” or “transport” molecules.
4. Glycolysis_: The First Stage of cellular respiration (the Energy- releasing Pathway).
These reactions take place entirely in the cytoplasm and occurs in two stages:
Two ATP molecules found in the
cytoplasm of the cell are used to activate
the incoming glucose molecule
and in a sense “traps” it in the cell to
ensure the concentration gradient is
maintained and to rearrange the molecule
to make it more symmetrical (balanced)
so it will be easier to break in half.
B. Energy releasing_ Steps:
two three-carbon molecules called PGAL
that are further
modified by removing a hydrogen atom
from each and transferring them to two
NAD molecules forming NADH_
and replacing the hydrogen atoms with
two phosphate groups. Eventually the
phosphate groups are removed and
transferred to ADP molecules forming a
total of four ATP molecules and two
molecules of pyruvate
(pyruvic acid) as the end products of this
series of reactions.
The PGAL molecules are important intermediate molecules as they serve as a location where part of the triglyceride molecules can enter the pathway to be used to produce ATP energy. And the 2PGA or BPG molecules are important as they influence whether hemoglobin molecules in red blood cells will keep or release oxygen to the tissue.
When ATP molecules are produced in the absence of oxygen by transferring phosphate groups from the substrate molecules (reactants) to ADP molecules, the
process is called substrate-level PHOSPHORYLATION.
In review: The following are the key points to remember about Glycolysis.
The initial reactant was Glucose. Two molecules of ATP were added helping to trap and rearrange the molecule to make it easier to break
in half. Eventually 4 ATP molecules were produced, resulting in a net gain
overall of 2 ATP, and 2 NADH molecules (to be used later by the
mitochondria to produce even more ATP) as well as two molecules of the final
product . These series of reactions do not rely on the presence of oxygen, so they can occur in an anaerobic situation when oxygen levels are low.
5. Krebs CYCLE (Citric Acid Cycle): The Second Stage of cellular respiration (the Energy-releasing Pathway).
These reactions take place entirely in the inner compartment or inner membrane space (matrix) of the mitochondria and also occur in two stages:
A. The Acetal Coa Formation Stage:
production of 2 pyruvate (pyruvic acid)
molecules; therefore all reactions in this step are
doubled. The pyruvate molecules are oxidized into
two 2-carbon molecules with the help of a special
enzyme helper called “Coenzyme A” producing two
molecules of Acetyl Co-A. In the process, a total of
another 2 NADH molecules were produced as
well as 2 CO2 molecules that are waste products.
Because there were two Acetyl-CoA molecules
produced in preparing to enter the cycle, all
reactions here are also doubled. The remaining hydrogen
atoms are removed and
given to the “carrier molecules” NAD+ and FAD
producing an additional 6 NADH and 2
FADH2 molecules that will later be
used by the mitochondria to produce even
more ATP molecules. In addition to the
“carrier molecules” produced, an additional 4
CO2 molecules and 2 ATP are
produced by a process called substrate-level
phosphorylation.
Even though these series of reactions do not rely on the presence of oxygen directly, the main products produced (NADH and FADH2) will be sent to the last stage of cellular respiration that DOES require oxygen and therefore Krebs Cycle will only occur in an aerobic situation when oxygen levels are high.
In review: The following are the key points to remember about Krebs Cycle.
The process began with two molecules of pyruvates that were produced by the break-down of one glucose molecule so all reactions are actually doubled (once for each of these molecules). In the initial reactions,
two hydrogen atoms were removed forming two molecules of and
two molecules of NADH that are waste products, as well as two molecules
of CO2 that will enter Krebs cycle proper. During the
final series of reactions, 2 more NADH will be produced for a total
of 6 NADH, 2 FADH2, four more molecules of co2
that are waste products for a total of 6 CO2 as well as 2 ATP by a process called substrate-level phosphorylation.
6.oxidative PHOSPHORYLATION: The third Stage of cellular respiration (the Energy-releasing Pathway), is also known as the electron transport chain (since it involves the removal of electrons from the hydrogen atoms), or oxidative phosphorylation (since oxygen is required to make ATP).
A. These reactions takes place along the inner-mitochondrial membrane. The coenzyme carrier molecules NADH and FADH2 deliver the Hydrogen atoms to specialized enzymes (embedded in the membrane) that will remove the electrons
and use the potential energy to drive the production of ATP molecules.
B. The “Chemiosmosis Theory” attempts to explain how this process occurs.
1. When the hydrogen atoms are delivered to the specialized enzymes in the membrane, the enzymes remove the electron and as it is passed along from enzyme to enzyme the action produces enough energy to transfer the unbound hydrogen ions (H+1) to the outer compartment of the mitochondria creating a concentration gradient of hydrogen ions.
2. Also embedded in the inner-mitochondrial membrane are very specialized
transporter (channel) proteins called ATP synthase that allow the Hydrogen ions (H+1) that have a high concentration in the outer compartment to move down their concentration gradient into the inner compartment. The movement of the H+1 ions through these proteins provides the needed energy to drive the phosphorylation of ADP into ATP.
3. At the end of the electron transport system the electrons need to go somewhere. Remember from chapter 2 that some elements are “takers” of
electrons and some are “givers”. The element oxygen was classified as a taker
. Oxygen atoms take the electrons from the transporter enzymes becoming a negative ion (O-2) at which point it is immediately attracted to some of the hydrogen ions (H+1) and the two join
together to produce a molecule of water . To put it another way, oxygen
is the final electron acceptor and water is the final
product along with the ATP molecules.
7. Anaerobic Energy-Releasing Pathways:
A. Unlike aerobic respiration, the anaerobic pathways do not use oxygen in the last steps as the final electron acceptor; their final steps have the important function of regenerating NAD+ “carrier molecules.
1. Without an adequate supply of oxygen there would be no place for the electrons to go, so the electrons would “build up” in the electron transport chain, and soon the NADH and FADH2 would not be able to release their Hydrogen atoms, essentially shutting down this stage.
2. If the carrier molecules were not able to release the hydrogen, soon there would be no more available to “take” the hydrogens released in Krebs cycle, essentially shutting down that stage as well.
3. If Krebs cycle “shuts down” it seems logical that Glycolysis would shut down as well; however, the cell must have at least some ATP to stay alive!
B. Without an adequate supply of oxygen, only the first stage (Glycolysis) can occur. Each glucose molecule will produce a total of only 2ATP rather than 36 ATP when oxygen is readily available. This is not a very good use of glucose but 2 ATP molecules are better than none and this works fine for a short time. The problem is that the NADH produced have no where to go (remember the electron transfer chain is shut down without oxygen) and will eventually need to be recycled.
C. There are two processes that can recycle the NADH back into NAD+1.
1. Alcohol FERMENTATION:
a. This process is used by yeast and other anaerobic organisms to produce energy when oxygen levels are low.
b. This process also uses Glycolysis as the first step to produce 2 ATP, but the rest of the energy-releasing pathways are shut down so because there is no place to send the Pyruvic acid molecules, and the supply of NADH will run out, the cell uses these molecules to produce Carbon dioxide gas and Ethanol (ethyl alcohol).
d. Ethanol in large quantities is toxic and eventually the cells will die, which is why this method is NOT used by our bodies to generate more NAD+ when oxygen levels are low.
2. Lactate FERMENTATION:
a. This process occurs especially in muscle cells when the demand for energy is intense but brief, as in sprinting or lifting weights.
b. Special enzymes remove the hydrogen atoms from the NADH and give it back to the pyruvate molecule converting it into a lactate (lactic acid) molecule, and in the process the NAD+ is regenerated so glycolysis can continue.
d. Some muscle cells (muscle fibers) must be able to stay contracted for a long period of time to keep the body or body part upright, such as your back and neck muscles or be able to contract repeatedly for an extended period of time, as in the leg muscles of marathon runners. Cells capable
of these activities are called slow twitch muscle fibers, and make ATP only by aerobic respiration. This means they must have a
large number of mitochondria , and a constant supply of oxygen. Muscles containing this type of cells appear dark in color due to the increased blood supply and the presence of a protein that stores the oxygen until needed, hence the term “dark” meat.
e. Some muscle cells (muscle fibers) must be able to contract very quickly and forcefully, as in jumping, throwing a “fast pitch” ball or a reflex reaction as when touching a hot object. Cells capable of these activities
are called fast twitch muscle fibers, and use the process of Lactate Fermentation (anaerobic respiration) to make ATP; therefore these cells have very few mitochondria. The pathway makes ATP very quickly but not for very long. It is not an effective use of glucose (2 ATP verses 36 ATP). Muscles containing this type of cells do not have a rich blood supply and do not store oxygen, so appear light in color, hence the term “light” or “white” meat.
8. Alternative Energy Sources in the Human Body
A. This chapter has concentrated on the use of glucose for the production of ATP energy because it is the body’s preference as an energy source. When glucose levels are high, the cell makes as much ATP as possible to have it available if the cell should need it in the future. Once the ATP levels get high enough (especially in the muscle and liver cells), the glucose is used to make other molecules like glycogen and triglycerides to store the energy for later use.
1. Energy from GLYCOGEN stored in the liver and skeletal muscles:
a. When blood sugar levels decline, the pancreas releases the hormone glucagon (glucose is almost gone).
b. Liver cells are stimulated to break down the glycogen back into glucose and release it to the blood. Muscle cells are also stimulated to break down the glycogen, but they keep the glucose for themselves and do not release it into the blood.
c. Polysaccharides like glycogen and starch have the potential of generating 4 kilocalories of energy per gram.
2. Energy from FATS (Triglycerides) stored in adipose cells:
a. The triglycerides are broken down into their component parts:
1. The 3-carbon glycerol backbone enters at the half-way point of
glycolysis and continues through the rest of the cellular respiration pathways as though it started out as glucose.
2. The fatty acid molecules (tails) are broken down with the help of a
coenzyme into acetyl-Co A molecules that enter Krebs cycle
and continue through the rest of the cellular respiration pathways as though they started out as glucose.
b. Fats have a much higher concentration of hydrogen atoms than carbohydrates and proteins and therefore more electrons and more energy potential.
c. They are also much less dense (are lighter) so gram for gram fats have the potential of generating more than twice the amount of energy as either carbohydrates or proteins, in fact fats have the potential of generating
9 kilocalories per gram.
3. Energy from Proteins:
a. The proteins are first broken down into their monomers (building blocks)
called Amino Acids.
b. The amino functional group is removed from the carbon atoms and excreted from the body as part of urine.
c. The carbon fragment that remains generally enters somewhere in kreb cycle
, depending on the number of carbon atoms in the group and continues through the pathway as though it started out as glucose.
d. Proteins like carbohydrates are able to produce 4 kilocalories of energy per gram.
B. During any 24-hour period, the body experiences two broad patterns of metabolic activity: the absorptive state and the postabsorptive state.
1. ABSORPTIVE STATE of metabolism: this is the period of time after consuming a meal (about 4 hours) when the body is absorbing nutrients from the digestive system. Some of the monomers are used immediately for energy; however the vast majority is stored for future use between meals, like when we are sleeping. The main reactions occurring at this time are classified
as _ (the building of large molecules from small ones) for growth of tissue and storage of energy reserves for future use.
2. POSTABSORPTIVE STATE of metabolism: this is the period of time when nutrients are NOT being absorbed from the digestive system and the body must rely on internal energy reserves. The main reactions occurring at this
time are classified as ___ (the breaking down of large molecules into smaller ones). Generally during this time, the goal is to maintain energy levels in the body. The glucose supply has dropped significantly so the body shifts from glucose catabolism to fatty acid and protein catabolism to obtain energy.
9. Just a few more points that need to be emphasized, then you’re done!
A. The overall reaction of cellular respiration is
1 C6H12O6 + 6 O2 → 6 CO2 + 6 H2O + 36 ATP
however no chemical reaction is ever 100% efficient. Our bodies are only able to capture about 40% of the total potential energy stored in a glucose molecule; the rest is lost as heat. This is why when you exercise, your cells need more energy so the rate of cellular respiration increases and more heat is produced, your body begins to overheat and you start sweating to try to lower the body temperature.
B. The energy-releasing pathways discussed in this chapter are also known as CELLULAR RESPIRATION. It is called this because the word respiration means the exchange of gases. The respiratory system in the body is responsible for taking in oxygen from the air and releasing carbon dioxide produced by the body. It has been shown that oxygen is critical to the efficient production of ATP from glucose, so cells must take in oxygen from the blood and use it to make ATP. It has also been shown that CO2 is produced as a waste product and the cell must eliminate it so in a sense the cells are “breathing” or exchanging gases just like the lungs.
C. All molecules (chemicals) have stored potential energy in the electrons located in their bonds. The goal of cellular respiration is to get at those electrons and use them to drive the production of ATP. To capture the electrons, hydrogen atoms must be separated from the carbon and oxygen so bonds must be broken, which releases heat. Remember, the hydrogen atom is the “weakest” of all the atoms in keeping the electron so it is the target of cellular respiration; if some other element was keeping the electron it may not give it back. The carrier molecules NAD+ and FAD are responsible for making sure the Hydrogen (with the electron) make it to their final destination (the electron transport chain).
D. Any substance that loses a hydrogen (or electron) is being OXIDIZED. Therefore glucose and all the intermediate molecules are being oxidized. Each of these molecules is losing some of their potential energy each time they lose or give away a hydrogen atom. The “carrier molecules” NAD+ and FAD are being REDUCED when they take the hydrogen atoms, which means they are “absorbing” more potential energy until they release the electron at the electron transport chain. The oxygen atom is the final electron acceptor, so it also is described as being REDUCED in the process of cellular respiration. Remember, any time a bond is formed, the substance is being REDUCED (more potential energy) and any time a bond is breaking, the substance is being OXIDIZED (less potential energy).
REVIEW ACTIVITIES:
10. Glycolysis is the first of three steps in cellular respiration. Review glycolysis by matching each phrase on the right with a term on the left. Some terms are used twice.
_ 2. Not involved in glycolysis
_ 3. Fuel molecule broken down in glycolysis
_ 4. Produced by substrate-level phosphorylation
_ 5. Invested to energize glucose molecule at start of process
_ 6. Reduced as glucose is oxidized
_ 7. Glucose converted to two molecules of this
_ 8. Assembled to make ATP
_ 9. “Splitting of sugar”
_ 10. Carries hydrogen and electrons from oxidation of
glucose
B. Pyruvic acid
C. ATP
D. NAD+
E. Glucose
F. Glycolysis
G. ADP and P
H. Oxygen
I. Intermediate
11. Check your overall understanding of cellular respiration by matching each of the phrases below with one of the stages of the process. Assume in each case that you originally started with one glucose molecule. (Some may require more than one letter.)
A. Glycolysis
B. Krebs’ Cycle and the Preparatory Steps
C. Electron Transport Chain (oxidative phosphorylation)
D. Lactic Acid Fermentation
_ 1. Generates most of the ATP formed by cellular respiration
_ 2. Begins the oxidation of glucose
_ 3. Occurs outside the mitochondrion
_ 4. Oxygen combines with H+ to form water molecules.
_ 5. Oxidizes NADH and FADH2, producing NAD+ and FAD
_ 6. Pyruvate is a reactant.
_ 7. Where electrons and hydrogen combine with O2 to form H2O
_ 8. Occurs along the inner mitochondrial membrane
_ 9. Generates most of the CO2 produced by cellular respiration
_ 10. FADH2 and NADH deliver hydrogen ions and electrons to this stage.
_ 11. ATP synthase makes ATP.
_ 12. Reduces NAD+ and FAD, producing NADH and FADH2
_ 13. Oxidative phosphorylation occurs to form ATP molecules.
_ 14. The carbon atoms in pyruvate leave as CO2 molecules.
_ 15. Oxidation and reduction reactions occur.
_ 16. Coenzyme A binds to a two-carbon acetyl group.
_ 17. Two NAD+ molecules form in the absence of oxygen.
_ 18. Two FADH2 and ten NADH are sent to this stage
_ 19. Lactic acid is an end product
_ 20. Water is one of the major products
_ 21. Occurs within the mitochondrion
_ 22. Two FADH2 and eight NADH form.
_ 23. Hydrogen ions collect in the mitochondrion’s outer compartment.
_ 24. Hydrogens and electrons are transferred to NAD+ and FAD.
_ 25. Two ATP molecules form by substrate-level phosphorylation.
_ 26. Oxygen is a major reactant
_ 27. No oxygen is required for ATP to be produced.
_ 28. Thirty-two to thirty-four ATPs are produced.
_ 29. NAD+ → NADH
_ 30. Carried out by enzymes in the matrix (fluid) of the mitochondrion
12. Choose the one most appropriate answer for each.
2. _ oxygen
3. _ mitochondrion
4. _ electron transport
phosphorylation
5. _ enzymes
6. _ ATP
7. _ glycolysis
8. _ aerobic respiration
9. _ cytoplasm
10. _ fermentation pathways
B. The overall process by which cells use oxygen to make the vast majority of the ATP needed
C. Site of glycolysis
D. Third and final stage of aerobic respiration; highest ATP yield generated
E. Oxygen is not the final electron acceptor
F. Catalyze each reaction step in the energy-releasing pathways
G. Second stage of aerobic respiration; pyruvate is broken down to CO2 and H2O
H. Site of the aerobic pathway
I. The final electron acceptor in aerobic pathways
J. The energy form that drives metabolic reactions
13. Compare the two mechanisms that generate ATP in cellular respiration—oxidative phosphorylation and substrate-level phosphorylation.
A. In what stage(s) of cellular respiration does each occur?
B. Where does each get the energy for making ATP?
C. Which one produces the most ATP under aerobic conditions?
D. Which one produces the most ATP under anaerobic conditions?
Sample test questions for chapter 8:
1. Cellular respiration oxidizes sugar and produces ATP in three main stages:
a. diffusion, passive transport and active transport
b. glycolysis, lactic acid fermentation, alcoholic fermentation
c. Krebs cycle, acetyl CoA, ATP
d. Glycolysis, Krebs cycle, electron transport chain
2. During “REDOX” reactions
a. the loss of electrons from one substance is called reduction
b. a substance that gains electrons is said to be oxidized
c. electrons are lost from one substance and added to another substance
d. protons from one molecule replace the electrons lost from another molecule
e. A, B and C
3. Which of the following statements differentiates substate-level phosphorylation from chemiosmotic (oxidative) phosphorylation?
a. a phosphate group is transferred directly from a metabolic intermediate to ADP forming ATP
b. it does not require the electron transport chain
c. it can occur in the absence of oxygen
d. it can occur outside the mitochondria
e. all of the above
4. During which of the following phases of cellular respiration does substrate-level phosphorylation take place?
a. glycolysis
b. the Krebs cycle
c. electron transport chain
d. both A and B
5. The end products of glycolysis include
a. FADH2
b. NADH
c. Acetyl CoA
d. glucose
e. CO2
6. In the respiratory electron transport chain, electrons pass from one electron transport molecule to another and are finally accepted by
a. a molecule of CO2
b. a molecule of water
c. an oxygen atom
d. ADP
e. ATP
7. When a fatty acid molecule is used for aerobic respiration, it is converted into , which is fed into .
a. glucose……..glycolysis
b. glyceraldehyde-3-phosphate…….glycolysis (partway through)
c. acetyl CoA…….the Krebs cycle
8. The body’s preferred source of energy is/are
a. triglycerides
b. proteins
c. glycerol
d. macrominerals
e. glucose
9. The end product(s) of the electron transport chain is/are
a. ATP
b. ATP and CO2
c. pyruvic acid
d. ATP and water
e. ATP and O2
10. Each NADH is capable of producing how many ATP from the Electron Transport Chain?
a. 1
b. 2
c. 3
d. 30
e. 36
11. Under anaerobic conditions, muscle cells produce __ from the glucose as it is producing ATP energy.
a. ethyl alcohol
b. pyruvate
c. lactic acid
d. glycogen
12. Which of the following processes occurs inside the mitochondria?
a. Kreb’s Cycle
b. Electron Transport Chain
c. Glycolysis
d. A and B
e. A, B and C
13. In which of the following processes does substrate level phosphorylation occur?
a. Kreb’s Cycle
b. Glycolysis
c. Electron Transport Chain
d. A and B
e. A, B and C
14. Most of the ATP is produced
a. by substrate level phosphorylation
b. by oxidative phosphorylation
15. Which has the potential of producing the most ATP?
a. glucose
b. amino acid
c. fatty acid